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Key Documents

Safety Information

133019

Sigma-Aldrich

Bis(2-hydroxypropyl)amine

95%

Synonym(s):

1,1′-Iminodi-2-propanol, Diisopropanolamine

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About This Item

Linear Formula:
NH[CH2CH(OH)CH3]2
CAS Number:
Molecular Weight:
133.19
Beilstein:
605363
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

95%

bp

249-250 °C/745 mmHg (lit.)

mp

42-45 °C (lit.)

solubility

alcohol: miscible
hydrocarbons: insoluble
toluene: slightly soluble
water: miscible

density

1.004 g/mL at 25 °C (lit.)

SMILES string

CC(O)CNCC(C)O

InChI

1S/C6H15NO2/c1-5(8)3-7-4-6(2)9/h5-9H,3-4H2,1-2H3

InChI key

LVTYICIALWPMFW-UHFFFAOYSA-N

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General description

Bis(2-hydroxypropyl)amine(Diisopropanolamine) is a flexible amino-alcohol ligand and induces the dimerisation of two trinuclear FeIII complexes to form the hexanuclear clusters.

Application

Bis(2-hydroxypropyl)amine(Diisopropanolamine) was used during the sulfinol process to remove sour gases such as hydrogen sulfide and carbonyl sulfide from natural gas.

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

275.0 °F - closed cup

Flash Point(C)

135 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

133019-1KG:
133019-250G:
133019-25KG:
133019-5G:
133019-BULK:
133019-VAR:


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Leigh F Jones et al.
Dalton transactions (Cambridge, England : 2003), (20)(20), 3344-3352 (2005-09-30)
The synthesis, crystal structures and magnetic properties of two hexanuclear Fe(6) clusters of general formula [Fe(6)(O)(2)(OH)(2)(O(2)CR)(10)(dipaH(2))(2)].xMeCN.yH(2)O (R = Ph, x= 5.5, y= 1 (1), R = C(Me)(3), x= 2, y= 3 (2)) are reported. The presence of the flexible amino-alcohol
Uptake of sulfolane and diisopropanolamine (DIPA) by cattails (Typha latifolia).
Doucette WJ, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 81(1), 41-49 (2005)
K A Johnson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45(10), 1838-1845 (2007-05-18)
The repeated dose oral and dermal toxicity of diisopropanolamine (DIPA) was evaluated in rats and compared to the reported toxicity of the related secondary alcohol amine, diethanolamine (DEA). Fischer 344/DuCrl rats were given up to 750 mg/kg/day by dermal application
L M Gieg et al.
Canadian journal of microbiology, 45(5), 377-388 (1999-08-14)
Diisopropanolamine (DIPA) is a "sweetening agent" used to remove hydrogen sulfide from sour natural gas, and it is a contaminant at some sour gas treatment facilities in western Canada. To investigate the biodegradation of this alkanolamine, 14C-DIPA was used in
K Yamamoto et al.
Carcinogenesis, 10(9), 1607-1611 (1989-09-01)
The carcinogenic activity of endogenously synthesized N-nitrosobis(2-hydroxypropyl)amine (BHP) was investigated in male Wistar rats administered bis(2-hydroxypropyl)amine (BHPA) mixed in powder diet at a concentration of 1%, and sodium nitrite (SN) dissolved in distilled water at concentrations of 0.15 and 0.3%

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